Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907583Generated: October 30, 2026

Chloromethyl Methyl Ether → 1-Bromo-4-methoxy-2-(methoxymethoxy)benzene

https://huagongshe.com/reaction/907583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-methoxyphenolHCID 13493839—
SolventAcetoneHCID 180—
Product1-Bromo-4-methoxy-2-(methoxymethoxy)benzeneHCID 1482703792%

Reaction Conditions

Temperature23 °C

Reaction Steps

Protected haloorganoboronic acid 14 was synthesized by a multi-step process. To a stirred mixture of 2-bromo-5-methoxyphenol (Albert, 2002) (2.19 g, 10.8 mmol) and K2CO3 (4.46 g, 32.3 mmol) in acetone (55 mL) was added chloromethyl methyl ether (1.63 mL, 21.5 mmol). The mixture was refluxed for 3 h and then allowed to cool to 23° C. The mixture was filtered and the filtrate was concentrated in vacuo. The crude product was then purified by flash chromatography (SiO2, hexanes:EtOAc 95:5) to provide 2-bromo-5-methoxy-1-methoxymethoxybenzene as a colorless liquid (2.43 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013203B2
Source datasetuspto-grants-2011_09
ORD IDord-25bbc4f02c614ebf995f459f1a658750
Source noteuspto-grants-2011_09